{"title":"特发性阴囊钙质沉着症的发病与表皮囊肿有关吗?一例印度农村病例报告及文献综述","authors":"M. Krishna, S. Dayal","doi":"10.4103/jewd.jewd_32_21","DOIUrl":null,"url":null,"abstract":"Idiopathic calcinosis cutis is characterized by multiple nodules present on scrotal skin. They are usually seen in young adults and present as painless, asymptomatic, round, and firm nodules. A 30-year-old male presented with painless, multiple scrotal nodules. The serum levels of calcium, phosphorus, calcitonin, and parathyroid hormone were within normal limits. There was also no history of trauma. Clinically, it was diagnosed as sebaceous cyst. Fine-needle aspiration cytology examination was suggestive of epidermal inclusion cyst. Histopathology examination confirmed the diagnosis of idiopathic scrotal calcinosis cutis, thus suggesting that the dystrophic calcification of epidermal inclusion may be an initiating event in the pathogenesis of the idiopathic scrotal calcinosis cutis. The documentations regarding the association of idiopathic calcinosis cutis with epidermal cyst are not enough. Hence, this case report may enrich the scanty existing data.","PeriodicalId":17298,"journal":{"name":"Journal of the Egyptian Women's Dermatologic Society","volume":"18 1","pages":"219 - 221"},"PeriodicalIF":0.3000,"publicationDate":"2021-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Idiopathic Scrotal calcinosis cutis – does its pathogenesis link with epidermal cyst? A case report with review of literature from rural India\",\"authors\":\"M. Krishna, S. Dayal\",\"doi\":\"10.4103/jewd.jewd_32_21\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Idiopathic calcinosis cutis is characterized by multiple nodules present on scrotal skin. They are usually seen in young adults and present as painless, asymptomatic, round, and firm nodules. A 30-year-old male presented with painless, multiple scrotal nodules. The serum levels of calcium, phosphorus, calcitonin, and parathyroid hormone were within normal limits. There was also no history of trauma. Clinically, it was diagnosed as sebaceous cyst. Fine-needle aspiration cytology examination was suggestive of epidermal inclusion cyst. Histopathology examination confirmed the diagnosis of idiopathic scrotal calcinosis cutis, thus suggesting that the dystrophic calcification of epidermal inclusion may be an initiating event in the pathogenesis of the idiopathic scrotal calcinosis cutis. The documentations regarding the association of idiopathic calcinosis cutis with epidermal cyst are not enough. Hence, this case report may enrich the scanty existing data.\",\"PeriodicalId\":17298,\"journal\":{\"name\":\"Journal of the Egyptian Women's Dermatologic Society\",\"volume\":\"18 1\",\"pages\":\"219 - 221\"},\"PeriodicalIF\":0.3000,\"publicationDate\":\"2021-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Egyptian Women's Dermatologic Society\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/jewd.jewd_32_21\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"DERMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Egyptian Women's Dermatologic Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/jewd.jewd_32_21","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"DERMATOLOGY","Score":null,"Total":0}
Idiopathic Scrotal calcinosis cutis – does its pathogenesis link with epidermal cyst? A case report with review of literature from rural India
Idiopathic calcinosis cutis is characterized by multiple nodules present on scrotal skin. They are usually seen in young adults and present as painless, asymptomatic, round, and firm nodules. A 30-year-old male presented with painless, multiple scrotal nodules. The serum levels of calcium, phosphorus, calcitonin, and parathyroid hormone were within normal limits. There was also no history of trauma. Clinically, it was diagnosed as sebaceous cyst. Fine-needle aspiration cytology examination was suggestive of epidermal inclusion cyst. Histopathology examination confirmed the diagnosis of idiopathic scrotal calcinosis cutis, thus suggesting that the dystrophic calcification of epidermal inclusion may be an initiating event in the pathogenesis of the idiopathic scrotal calcinosis cutis. The documentations regarding the association of idiopathic calcinosis cutis with epidermal cyst are not enough. Hence, this case report may enrich the scanty existing data.
期刊介绍:
The Journal of The Egyptian Women''s Dermatologic Society (JEWDS) was founded by Professor Zenab M.G. El-Gothamy. JEWDS is published three times per year in January, May and September. Original articles, case reports, correspondence and review articles submitted for publication must be original and must not have been published previously or considered for publication elsewhere. Their subject should pertain to dermatology or a related scientific and technical subject within the field of dermatology.